(B) Alkenes undergo electrophilic addition reactions. $HOCl$ acts as a source of the electrophile $Cl^{+}$. In the first step,the electrophile $Cl^{+}

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(B) Alkenes undergo electrophilic addition reactions. $HOCl$ acts as a source of the electrophile $Cl^{+}$. In the first step,the electrophile $Cl^{+}$ attacks the double bond of propene to form a cyclic chloronium ion intermediate. Subsequently,the nucleophile $OH^{-}$ attacks the more substituted carbon atom to form the final product,chlorohydrin.

Class 11 Chemistry Hydrocarbons Alkene

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The reaction of propene with $HOCl$ proceeds via the addition of

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A
$H^{+}$ in the first step
B
$Cl^{+}$ in the first step
C
$OH^{-}$ in the first step
D
$Cl^{+}$ and $OH^{-}$ in a single step

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Class 11

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Hydrocarbons

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Alkene

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IIT 2001 Paper All IIT years →

Addition of $HCl$ to vinyl chloride $(CH_2=CHCl)$ gives $1, 1-$dichloroethane $(CH_3-CHCl_2)$ because of:

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When an alcoholic solution of ethylene dibromide $(Br-CH_2-CH_2-Br)$ is heated with granulated zinc,the compound formed is:

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Which of the following compounds does not follow the Markovnikov rule when reacting with $HBr$?

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The product of the following reaction is:
$CH_3-CH=CH-CH_3 \xrightarrow{MCPBA, CH_2Cl_2} \text{Product}$

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What is the major product formed by the reaction of $2$-methylpropene with $HBr$?

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The reaction of propene with $HOCl$ proceeds via the addition of

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Addition of $HCl$ to vinyl chloride $(CH_2=CHCl)$ gives $1, 1-$dichloroethane $(CH_3-CHCl_2)$ because of:

When an alcoholic solution of ethylene dibromide $(Br-CH_2-CH_2-Br)$ is heated with granulated zinc,the compound formed is:

Which of the following compounds does not follow the Markovnikov rule when reacting with $HBr$?

The product of the following reaction is:$CH_3-CH=CH-CH_3 \xrightarrow{MCPBA, CH_2Cl_2} \text{Product}$

What is the major product formed by the reaction of $2$-methylpropene with $HBr$?

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The product of the following reaction is:
$CH_3-CH=CH-CH_3 \xrightarrow{MCPBA, CH_2Cl_2} \text{Product}$